JCI Insight. 2017 Nov 16;2(22). doi: 10.1172/jci.insight.92724.
A role of B cells in multiple sclerosis (MS) is well established, but there is limited understanding of their involvement during active disease. Here, we examined cerebrospinal fluid (CSF) and peripheral blood (PB) B cells in treatment-naive patients with MS or high-risk clinically isolated syndrome. Using flow cytometry, we found increased CSF lymphocytes with a disproportionate increase of B cells compared with T cells in patients with gadolinium-enhancing (Gd+) lesions on brain MRI. Ig gene heavy chain variable region (Ig-VH) repertoire sequencing of CSF and PB B cells revealed clonal relationships between intrathecal and peripheral B cell populations, which could be consistent with migration of B cells to and activation in the CNS in active MS. In addition, we found evidence for bystander immigration of B cells from the periphery, which could be supported by a CXCL13 gradient between CSF and blood. Understanding what triggers B cells to migrate and home to the CNS may ultimately aid in the rational selection of therapeutic strategies to limit progression in MS.
B 细胞在多发性硬化症(MS)中的作用已得到充分证实,但人们对其在疾病活动期的参与仍知之甚少。在这里,我们检查了未经治疗的 MS 患者或高风险临床孤立综合征患者的脑脊液(CSF)和外周血(PB)B 细胞。通过流式细胞术,我们发现与 T 细胞相比,MRI 上有钆增强(Gd+)病变的患者的 CSF 淋巴细胞增多,其中 B 细胞不成比例地增加。CSF 和 PB B 细胞的 Ig 基因重链可变区(Ig-VH)库测序显示,鞘内和外周 B 细胞群之间存在克隆关系,这可能与 B 细胞向中枢神经系统迁移和在活跃的 MS 中激活相一致。此外,我们发现证据表明 B 细胞从外周旁观移民,这可能得到 CSF 和血液之间 CXCL13 梯度的支持。了解是什么引发 B 细胞迁移并归巢到中枢神经系统,最终可能有助于合理选择治疗策略,以限制 MS 的进展。